PAH: Pulmonary Arterial Hypertension (PAH)-CHD | |
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10:00 – 10:20 | Pathophysiology of pulmonary hypertension in congenital heart disease Maurice Beghetti, Switzerland |
10:20 – 10:40 | Operability in PAH-CHD AntonioAugusto Lopes, Brazil |
10:40 – 11:00 | Management of Eisenmenger syndrome Gul Sagin Saylam, Turkey |
11:00 – 11:20 | Evaluation and management of pulmonary hypertension in children with end stage left heart failure Robert Weintraub, Australia |
11:20 – 11:40 | PAH in the child with Down Syndrome Mary Mullen, US |
11:40 – 12:00 | Persistent postoperative PAH Gu Hong, China |